ES2 SPINAL SYSTEMRecalls & reported problems across all models
Stryker Corporation · 54 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 218
- Deaths reported
- 0
- Injuries reported
- 82
- Recalls
- 0
We found 54 models of ES2 SPINAL SYSTEM by Stryker Corporation in the FDA's device registry (GUDID). Together they are named in 218 adverse event reports in the FDA's MAUDE database, received between Feb 24, 2016 and Sep 23, 2026 — classified as 82 injuries, 136 malfunctions.
The most frequently reported specific device problem is “Fracture” (102 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported ES2 SPINAL SYSTEM problems
Device problems
- Fracture102
- Break53
- Migration39
- Device Dislodged or Dislocated25
- Material Integrity Problem23
- Detachment of Device or Device Component17
- Detachment Of Device Component15
- Mechanical Problem15
Patient problems
- No Known Impact Or Consequence To Patient72
- No Clinical Signs, Symptoms or Conditions71
- Injury49
- No Code Available19
- No Consequences Or Impact To Patient17
- Insufficient Information16
- Device Embedded In Tissue or Plaque14
- Pain12
ES2 SPINAL SYSTEM models
54 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ES2 SPINAL SYSTEM 48280145ORTHOPEDIC MANUAL SURGICAL INSTRUMENT31 reports
- ES2 SPINAL SYSTEM 482802745Orthosis, spinal pedicle fixation, for degenerative disc disease21 reports
- ES2 SPINAL SYSTEM 48280232ORTHOPEDIC MANUAL SURGICAL INSTRUMENT21 reports
- ES2 SPINAL SYSTEM 482802740APPLIANCE, FIXATION, SPINAL INTERLAMINAL20 reports
- ES2 SPINAL SYSTEM 482802540ORTHOSIS, SPINAL PEDICLE FIXATION12 reports
- ES2 SPINAL SYSTEM 482804645Orthosis, spondylolisthesis spinal fixation12 reports
- ES2 SPINAL SYSTEM 482802645APPLIANCE, FIXATION, SPINAL INTERLAMINAL9 reports
- ES2 SPINAL SYSTEM 482802650Orthosis, spinal pedicle fixation, for degenerative disc disease6 reports
- ES2 SPINAL SYSTEM 482804750Orthosis, spinal pedicle fixation, for degenerative disc disease6 reports
- ES2 SPINAL SYSTEM 482802640Orthosis, spondylolisthesis spinal fixation4 reports
- ES2 SPINAL SYSTEM 482802750Orthosis, spondylolisthesis spinal fixation4 reports
- ES2 SPINAL SYSTEM 482804650APPLIANCE, FIXATION, SPINAL INTERLAMINAL4 reports
- ES2 SPINAL SYSTEM 482804745Orthosis, spinal pedicle fixation, for degenerative disc disease4 reports
- ES2 SPINAL SYSTEM 482804760Orthosis, spinal pedicle fixation, for degenerative disc disease4 reports
- ES2 SPINAL SYSTEM 482802880Orthosis, spinal pedicle fixation, for degenerative disc disease4 reports
- ES2 SPINAL SYSTEM 48280310ORTHOPEDIC MANUAL SURGICAL INSTRUMENT3 reports
- ES2 SPINAL SYSTEM 482804740Orthosis, spinal pedicle fixation, for degenerative disc disease3 reports
- ES2 SPINAL SYSTEM 482802870APPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- ES2 SPINAL SYSTEM 48280311ORTHOPEDIC MANUAL SURGICAL INSTRUMENT3 reports
- ES2 SPINAL SYSTEM 48280155STIMULATOR, NERVE2 reports
- ES2 SPINAL SYSTEM 482807045Orthosis, spinal pedicle fixation, for degenerative disc disease2 reports
- ES2 SPINAL SYSTEM 482806060Orthosis, spinal pedicle fixation, for degenerative disc disease2 reports
- ES2 SPINAL SYSTEM 482802770Orthosis, spinal pedicle fixation, for degenerative disc disease2 reports
- ES2 SPINAL SYSTEM 482804660ORTHOSIS, SPINAL PEDICLE FIXATION2 reports
- ES2 SPINAL SYSTEM 482804755Orthosis, spinal pedicle fixation, for degenerative disc disease2 reports
- ES2 SPINAL SYSTEM 48280185STIMULATOR, NERVE2 reports
- ES2 SPINAL SYSTEM 48280081ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- ES2 SPINAL SYSTEM 48280233ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- ES2 SPINAL SYSTEM 48280165ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ES2 SPINAL SYSTEM 482807060ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482807065Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482807080Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482806050Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482806070Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482807480Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482806090ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482807180Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482802425ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482802440Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482802530APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 482802545Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482802550APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 482802655Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482802755Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482804540Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482804640ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482804735APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 482804435Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482804790APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 482804855Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482804870ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482804890ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 48280175ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ES2 SPINAL SYSTEM 48280090ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
Recent ES2 SPINAL SYSTEM adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026Detachment of Device or Device Component
A company representative reported that the tulip of an ES2 Integrated Blade Screw disengaged intra-operatively and that the screw was removed and replaced during the procedure. The procedure was completed successfully with a 20-minute surgical delay and no adverse consequence to the patient.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869301 ↗MalfunctionSep 17, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50810063 ↗MalfunctionSep 17, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50810058 ↗MalfunctionSep 17, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50810039 ↗MalfunctionSep 17, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50809863 ↗MalfunctionSep 8, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50680253 ↗InjurySep 8, 2026Migration
Patient problems: Insufficient Information
MAUDE report 50680247 ↗InjurySep 8, 2026Migration
Patient problems: Insufficient Information
MAUDE report 50680245 ↗InjurySep 8, 2026Migration
Patient problems: Insufficient Information
MAUDE report 50680242 ↗MalfunctionSep 1, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50551599 ↗MalfunctionSep 1, 2026Fracture
Patient problems: Insufficient Information
MAUDE report 50550582 ↗InjuryMar 25, 2026Insufficient Device Problem Information
InjuryMar 25, 2026Insufficient Device Problem Information
MalfunctionMar 24, 2026Migration
A HEALTH PROFESSIONAL REPORTED THAT A MANTIS REDUX BLOCKER AND AN ES2 ROD MIGRATED POST-OPERATIVELY. REVISION SURGERY HAS NOT TAKEN PLACE NOR BEEN SCHEDULED. NO ADVERSE CONSEQUENCES WERE REPORTED. THIS REPORT REPRESENTS THE ES2 ROD MIGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24682358 ↗InjuryMar 5, 2026Fracture
A COMPANY REPRESENTATIVE REPORTED THAT AN ES2 NITINOL K-WIRE BLUNT FRACTURED INTRA-OPERATIVELY. IT WAS FURTHER REPORTED THAT A LARGER INCISION WAS MADE INTRA-OPERATIVELY TO RETRIEVE THE FRACTURED COMPONENT AND ADDITIONAL X-RAYS WERE PERFORMED. THE PROCEDURE WAS COMPLETED WITH A FIVE MINUTE SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24519743 ↗
Other Stryker Corporation products
- RemB7 models · 3,073 reports
- Prime Series21 models · 1,548 reports · 2 recalls
- TARGET114 models · 1,077 reports
- ProCuity17 models · 368 reports · 13 recalls
- Spetzler-Malis20 models · 7 reports · 19 recalls
- SYNCHRO 28 models · 313 reports · 9 recalls
- Neptune E-SEP19 models · 412 reports · 7 recalls
- StrykeFlow4 models · 552 reports · 4 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page